26 research outputs found
Making Free Trade Fair
Philosophers have done very little work on what makes trade fair. Perhaps the most extensive discussion is Malgorzata Kurjanska and Mathias Risse’s article, “Fairness in Trade II: export subsidies and the fair trade movement.”2 In their article, Kurjanska and Risse consider the case for trade subsidies and the Fair Trade movement. They suggest that it is not permissible for developed countries to give their producers subsidies because doing so does not strike an appropriate balance between meeting the needs of the global poor and protecting domestic workers (Kurjanska and Risse, 2008: 34). Kurjanska and Risse also argue that the case for Fair Trade hinges, primarily, on whether or not it is part of the best development strategy for poor countries. They do not think Fair Trade is part of the best development strategy and, so, they believe purchasing Fair Trade certified goods is only acceptable because doing so does not constitute a large share of the market in traded goods. This chapter argues that the case against subsidies and Fair Trade Kurjanska and Risse present is much weaker than they make out. To the contrary, it argues that giving some subsidies and purchasing some Fair Trade certified goods may even be necessary to make trade fair. Section 11.2 starts by saying a few words about the normative framework Kurjanska and Risse adopt
Market Access Liberalization for Food and Agricultural Products: A General Equilibrium Assessment of Tariff-Rate Quotas
Design of indoor microstrip TV antenna for integrated services digital broadcast — Terrestrial (ISDB-T) signal reception at 677 MHz
Cotas tarifárias e o impacto sobre as exportações agrícolas brasileiras na União Européia
Este trabalho tem como objetivo avaliar os efeitos de cotas tarifárias adicionais para as exportações brasileiras de produtos agrícolas, com base na proposta européia de maio de 2004 no âmbito das negociações para um acordo de livre-comércio Mercosul- União Européia. A análise teórica do funcionamento dos três instrumentos da cota tarifária (seu volume e as tarifas intra e extracota) revela que, dependendo da demanda, apenas um deles efetivamente restringe as importações. Assim, a oferta de cotas adicionais não implica necessariamente um aumento equivalente na quantidade exportada. Na estimativa de ganho de receita deve ser considerada também a variação na renda da cota. Além disso, a administração da cota terá um papel crucial na alocação dessa renda. Caso seja o Mercosul a fazê-la, as estimativas indicam um aumento de US 252 milhões resultantes da apropriação das rendas das cotas e US 728 million in exports, of which US 476 million from exports. The sum of both is indeed close to the value of the additional quotas at current prices. If the administration goes to the EU, the gains will derive exclusively from the expansion in exports, which corresponds to 63.7% to the value of the quota
Response to antenatal cholecalciferol supplementation is associated with common vitamin D related genetic variants
Single-nucleotide polymorphisms (SNPs) in genes related to vitamin D metabolism have been associated with serum 25-hydroxyvitamin D [25(OH)D] concentration, but these relationships have not been examined following antenatal cholecalciferol supplementation.To determine whether SNPs in DHCR7, CYP2R1, CYP24A1, and GC are associated with the response to gestational cholecalciferol supplementation.Within-randomization group analysis of the Maternal Vitamin D Osteoporosis Study trial of antenatal cholecalciferol supplementation.Hospital antenatal clinics.In total, 682 women of white ethnicity (351 placebo, 331 cholecalciferol) were included. SNPs at rs12785878 (DHCR7), rs10741657 (CYP2R1), rs6013897 (CYP24A1), and rs2282679 (GC) were genotyped.1000 IU/d cholecalciferol from 14 weeks of gestation until delivery.25(OH)D at randomization and 34 weeks of gestation were measured in a single batch (Liaison; Diasorin, Dartford, UK). Associations between 25(OH)D and the SNPs were assessed by linear regression using an additive model [β represents the change in 25(OH)D per additional common allele].Only rs12785878 (DHCR7) was associated with baseline 25(OH)D [β = 3.1 nmol/L; 95% confidence interval (CI), 1.0 to 5.2 nmol/L; P < 0.004]. In contrast, rs10741657 (CYP2R1) (β = -5.2 nmol/L; 95% CI, -8.2 to -2.2 nmol/L; P = 0.001) and rs2282679 (GC) (β = 4.2 nmol/L; 95% CI, 0.9 to 7.5 nmol/L; P = 0.01) were associated with achieved 25(OH)D status following supplementation, whereas rs12785878 and rs6013897 (CYP24A1) were not.Genetic variation in DHCR7, which encodes 7-dehyrocholesterol reductase in the epidermal vitamin D biosynthesis pathway, appears to modify baseline 25(OH)D. In contrast, the response to antenatal cholecalciferol supplementation was associated with SNPs in CYP2R1, which may alter 25-hydroxylase activity, and GC, which may affect vitamin D binding protein synthesis or metabolite affinity
